Clinical Research Associate (CRA)2-5yrs immediate joiners

Role: Clinical Research Associate (CRA)

Work form home opportunity

Location: Navi Mumbai, India (Office Based)

Experience: 2–5 Years

Immediate joiners required

experience in monitoring global clinical trials - mandatory

Required Qualifications & Experience

- Bachelor's or Master's degree in Life Sciences, Pharmacy, or related field.

- 3–5 years of experience in clinical research, preferably within a CRO or pharmaceutical company.

- Good understanding of ICH-GCP guidelines and regulatory requirements.

- Experience on global clinical trials preferred.

- Strong communication and coordination skills.

- Ability to manage multiple tasks in a fast-paced environment

Key Responsibilities

- Support site identification, feasibility, and selection activities.

- Plan and conduct Site Initiation , Monitoring and Closeout visit

-Assist in study start-up activities including regulatory submissions, EC/IRB approvals, and site contracts.

- Perform remote monitoring activities and ensure data quality, accuracy, and completeness.

- Support Ethics Committee Submission and essential document collection.

- Track site performance, recruitment, and study timelines.

- Ensure compliance with study protocol, SOPs, ICH-GCP, and applicable regulations.

- Support site training and communication.

- Assist in preparation and maintenance of Trial Master File (TMF/eTMF).